Cargando…

Long non-coding RNA HANR as a biomarker for the diagnosis and prognosis of colorectal cancer

Previous work suggests that the long noncoding RNA HCC associated long non-coding RNA (HANR) is associated with hepatocellular carcinoma (HCC) progression, but its significance in the context of colorectal cancer (CRC) remains to be determined. Therefore, in this study we assessed the prognostic and...

Descripción completa

Detalles Bibliográficos
Autores principales:	Xu, Meng, Guo, Xu, Wang, Rong-Di, Zhang, Zhi-Hang, Jia, Yi-Mo, Sun, Xu
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer Health 2020
Materias:	3500
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7035088/ https://www.ncbi.nlm.nih.gov/pubmed/32049807 http://dx.doi.org/10.1097/MD.0000000000019066

Ejemplares similares

Prognostic significance of long intergenic non-protein-coding RNA 511expression in malignant tumors: A systematic review and meta-analysis
por: Chen, Ming, et al.
Publicado: (2020)

NIFK as a potential prognostic biomarker in colorectal cancer correlating with immune infiltrates
por: Tan, Lin, et al.
Publicado: (2023)

Identification and verification of m6A-related miRNAs correlated with prognosis and immune microenvironment in colorectal cancer
por: Qiu, Xinze, et al.
Publicado: (2023)

Prenatal diagnosis of chromosome 18 long arm deletion syndrome by high-throughput sequencing: Two case reports
por: Bai, Xuechun, et al.
Publicado: (2021)

CT perfusion imaging parameters and serum miR-106a-5p predict short- and long-term prognosis in acute cerebral infarction patients after intravenous thrombolysis
por: Du, Juan, et al.
Publicado: (2023)

Association of several loci of SMAD7 with colorectal cancer: A meta-analysis based on case–control studies
por: Xiao, Qiang, et al.
Publicado: (2023)

Prognostic evaluation of microRNA-210 in various carcinomas: Evidence from 19 studies
por: Liu, Yincheng, et al.
Publicado: (2017)

Missed diagnosis of lissencephaly after prenatal diagnosis: A case report
por: Liu, Mengna, et al.
Publicado: (2023)

NOTCH3 Gene Polymorphism is Associated With the Prognosis of Gliomas in Chinese Patients
por: Shen, Zhipeng, et al.
Publicado: (2015)

High expression of MMP28 indicates unfavorable prognosis in pancreatic cancer
por: Chen, Zhitao, et al.
Publicado: (2021)

Genotype and clinical phenotype analysis of a Family with Kennedy disease
por: Cai, Ben-Chi, et al.
Publicado: (2023)

Genetic variations associated with telomere length affect the risk of gastric carcinoma
por: Lili, Ma, et al.
Publicado: (2020)

The important role of MDM2, RPL5, and TP53 in mycophenolic acid-induced cleft lip and palate
por: Lin, Yangyang, et al.
Publicado: (2021)

Pharmacogenetic and case–control study on potassium channel related gene variants and genetic generalized epilepsy
por: Qu, Jian, et al.
Publicado: (2017)

An elective radiation dose of 46 Gy is feasible in nasopharyngeal carcinoma treated by intensity-modulated radiotherapy: A long-term follow-up result
por: Hung, Tsung-Min, et al.
Publicado: (2017)

PD-1 rs2227982 Polymorphism Is Associated With the Decreased Risk of Breast Cancer in Northwest Chinese Women: A Hospital-Based Observational Study
por: Ren, Hong-Tao, et al.
Publicado: (2016)

Transthyretin-related hereditary amyloidosis with recurrent vomiting and renal insufficiency as the initial presentation: A case report
por: Xu, Jing, et al.
Publicado: (2017)

Polymorphism in the IL4R gene and clinical features are associated with glioma prognosis: Analyses of case-cohort studies
por: Jin, Tian bo, et al.
Publicado: (2016)

Identification of a cancer-associated fibroblast classifier for predicting prognosis and therapeutic response in lung squamous cell carcinoma
por: Lai, Xixi, et al.
Publicado: (2023)

Genetic Variation in Metastasis-Associated in Colon Cancer-1 and the Risk of Breast Cancer Among the Chinese Han Population: A STROBE-Compliant Observational Study
por: Dai, Zhi-Jun, et al.
Publicado: (2016)

Genetic Variations in Key MicroRNAs are Associated With the Survival of Nonsmall Cell Lung Cancer
por: Wu, Shuangshuang, et al.
Publicado: (2015)

Identification of HIV-1-specific cascaded microRNA-mRNA regulatory relationships by parallel mRNA and microRNA expression profiling with AIDS patients after antiviral treatment
por: Shen, Fangyuan, et al.
Publicado: (2021)

The cGAS-STING pathway-related gene signature can predict patient prognosis and immunotherapy responses in prostate adenocarcinoma
por: Zhuo, Xingxing, et al.
Publicado: (2022)

Molecular diagnosis of sex chromosome mosaics in fetal amniotic cells
por: Fan, Zuqian, et al.
Publicado: (2021)

GALNT14 Genotype Predicts Postoperative Outcome of Stage III Colorectal Cancer With Oxaliplatin as Adjuvant Chemotherapy
por: Lin, Wey-Ran, et al.
Publicado: (2016)

Association between MDR1 C3435T polymorphism and colorectal cancer risk: A meta-analysis
por: Jin, Shan-Shan, et al.
Publicado: (2017)

Association between HIF-1α gene polymorphisms and lung cancer: A meta-analysis
por: Xu, Shuguang, et al.
Publicado: (2020)

A panel of 8 miRNAs as a novel diagnostic biomarker in pancreatic cancer
por: Deng, Benyuan, et al.
Publicado: (2020)

Aberrant gene expression pattern in the glycolysis-cholesterol synthesis axis is linked with immune infiltration and prognosis in prostate cancer: A bioinformatics analysis
por: Yuan, Yiwen, et al.
Publicado: (2022)

Diagnosis of Schaaf-Yang syndrome in Korean children with developmental delay and hypotonia
por: Ahn, Hyunji, et al.
Publicado: (2020)

Performance characterization of PCR-free whole genome sequencing for clinical diagnosis
por: Zhou, Guiju, et al.
Publicado: (2022)

TCF7L2, CASC8, and GREM1 polymorphism and colorectal cancer in south-eastern Romanian population
por: Mitroi, Anca Florentina, et al.
Publicado: (2023)

Identification of a novel X-linked arginine-vasopressin receptor 2 mutation in nephrogenic diabetes insipidus: Case report and pedigree analysis
por: Peng, Danxia, et al.
Publicado: (2019)

Identification of hub genes, key pathways, and therapeutic agents in Hutchinson–Gilford Progeria syndrome using bioinformatics analysis
por: Wang, Dengchuan, et al.
Publicado: (2020)

Antenatal screening and diagnosis of tuberous sclerosis complex by fetal echocardiography and targeted genomic sequencing
por: Gu, Xiaoyan, et al.
Publicado: (2018)

Expression of LINE-1 retrotransposon in early human spontaneous abortion tissues
por: Lou, Chao, et al.
Publicado: (2022)

GDF-15 (a biomarker for metformin) and the risk of COVID-19: A two-sample Mendelian randomization study
por: Wang, Ya, et al.
Publicado: (2023)

A novel EDA1 missense mutation in X-linked hypohidrotic ectodermal dysplasia
por: Wang, Xu, et al.
Publicado: (2020)

Prenatal diagnosis of 7q11.23 microdeletion: Two cases report and literature review
por: Lv, Xin, et al.
Publicado: (2023)

Integrating multiple microarray datasets to explore the significance of ferroptosis regulators in the diagnosis and subtype classification of osteoarthritis
por: Huang, Yue, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_k8bg835fl6o2j6cut3ijg84o6d